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FDA 510(k)

MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM

K-Number: K910217 · 1991-04-02

Decision Date1991-04-02
Product CodeFAP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Browne Medical Systems, Inc.. It received FDA 510(k) clearance on 1991-04-02 under 510(k) number K910217. The device is classified under product code FAP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM?

MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM is a medical device that received FDA 510(k) clearance on 1991-04-02. The listed applicant is Browne Medical Systems, Inc.. The 510(k) number is K910217.

When did MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM receive FDA 510(k) clearance?

MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM received FDA 510(k) clearance on 1991-04-02, under 510(k) number K910217.

Who is the listed applicant for MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM?

The FDA 510(k) record lists Browne Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM?

The FDA product code for MINIPRO 8100 URODYNAMIC MEASUREING SYSTEM is FAP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Browne Medical Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 7 devices →

Related Devices (Code: FAP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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